A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4609



Internal ID15196685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93067391..93111957hg38UCSC Ensembl
Outerchr7:92696704..92741270hg19UCSC Ensembl
Outerchr7:92534640..92579206hg18UCSC Ensembl
Outerchr7:92341355..92385921hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3844567
hg1944567
hg1844567
hg1744567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845
Supporting Variants
SamplesNA19129
Known GenesSAMD9
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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